Disease: Serum albumin measurement
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs740006
TMEM258
11 61790396 3 prime UTR variant T/C snv 7.6E-02 2
rs174538
TMEM258 ; MIR611 ; FEN1
0.701 0.440 11 61792609 5 prime UTR variant G/A snv 0.34 0.26 21
rs412334
FEN1 ; TMEM258 ; MIR611
11 61792789 5 prime UTR variant C/T snv 0.10 2
rs4246215
FADS2 ; FEN1
0.677 0.320 11 61796827 3 prime UTR variant G/C;T snv 29
rs174541
FADS2
1.000 0.080 11 61798436 intron variant T/C snv 0.29 8
rs174547
FADS2 ; FADS1
0.742 0.240 11 61803311 intron variant T/C snv 0.28 33
rs174548
FADS2 ; FADS1
0.851 0.160 11 61803876 5 prime UTR variant C/G;T snv 17
rs174550
FADS1 ; FADS2
0.925 0.160 11 61804006 5 prime UTR variant T/C snv 0.28 13
rs174556
FADS2 ; FADS1
0.925 0.160 11 61813163 intron variant C/T snv 0.26 7
rs968567
FADS2 ; FADS1
0.851 0.240 11 61828092 intron variant C/T snv 0.11 7
rs174570
FADS2
0.882 0.200 11 61829740 intron variant C/T snv 0.15 11
rs1535
FADS2
0.752 0.240 11 61830500 intron variant A/G snv 0.31 24
rs174574
FADS2
1.000 0.080 11 61832870 intron variant A/C snv 0.55 7
rs2845573
FADS2
1.000 0.040 11 61834436 intron variant A/G snv 9.7E-02 3
rs174575
FADS2
1.000 0.040 11 61834531 intron variant C/G snv 0.25 3
rs2727270
FADS2
11 61835765 intron variant C/T snv 0.12 2
rs2727271
FADS2
11 61835886 intron variant A/T snv 0.12 2
rs2524299
FADS2
11 61837310 intron variant A/T snv 0.17 2
rs2072114
FADS2
1.000 0.080 11 61837743 intron variant A/G snv 0.19 0.16 4
rs174579
FADS2
11 61838141 intron variant C/T snv 0.16 2
rs17156426
FADS2
11 61841851 intron variant A/G;T snv 2
rs174583
FADS2
0.807 0.320 11 61842278 intron variant C/T snv 0.35 16
rs174585
FADS2
11 61844222 intron variant G/A;T snv 2
rs17156442
FADS2
11 61846551 intron variant C/T snv 0.11 2
rs7935946
FADS2
11 61848070 5 prime UTR variant C/T snv 0.11 2